Influence of Dental Occlusion on the Performance of High Level Rowers (IODPR)
NCT ID: NCT03648125
Last Updated: 2018-08-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
7 participants
INTERVENTIONAL
2017-10-27
2017-11-22
Brief Summary
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Detailed Description
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The present study aims to evaluate the influence of dental occlusion on postural stability and the performance of high level rowers.
Our assumptions are as follows:
* Occlusal disturbance alters the muscular power developed by high level rowers
* occlusal disturbance alters the static postural stability of high level rowers
Conditions
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Study Design
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RANDOMIZED
SEQUENTIAL
BASIC_SCIENCE
NONE
Study Groups
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Rowing training session
Power tests, balance and tonicity tests are performed eyes opened and eyes closed :
* with artificial occlusal disturbance and
* without artificial occlusal disturbance
with artificial occlusal disturbance
A silicon artificial occlusal disturbance is made from a mould of the rowers mouth and placed in the mouth during the training session.
With artificial occlusal disturbance : Maximal Intercuspal Occlusion (MIO) with silicone splint increases the vertical dimension of occlusion of 1, 2 and 4 mm.
without artificial occlusal disturbance
The training session is performed without occlusal disturbance
Interventions
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with artificial occlusal disturbance
A silicon artificial occlusal disturbance is made from a mould of the rowers mouth and placed in the mouth during the training session.
With artificial occlusal disturbance : Maximal Intercuspal Occlusion (MIO) with silicone splint increases the vertical dimension of occlusion of 1, 2 and 4 mm.
without artificial occlusal disturbance
The training session is performed without occlusal disturbance
Eligibility Criteria
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Inclusion Criteria
* At least 15 years old;
* Training at the Centre de Ressources, d'Expertise et de Performance Sportive (CREPS) de Wattignies during the period from 01/09/2017 to 31/10/2017;
* Having at least 28 natural or prosthetic teeth in occlusion;
* Not having consumed alcohol in the last 24 hours before the recordings;
* whose parents have given free, informed and written consent for minors;
* Having given free and informed consent, in writing supplemented by the consent of at least one holder of parental authority, if he is a minor;
* Affiliated, himself or through his parents if he is a minor, to a social security scheme.
Exclusion Criteria
* Temporomandibular joint disorder (s) (pain and / or noise);
* Orofacial symptoms (headache, tinnitus, facial myalgia, bruxism);
* Dental and / or periodontal care in progress;
* Chronic pain requiring daily use of analgesics for more than three months;
* Pregnant or lactating woman;
* Concurrent participation in another study;
* Major persons subject to legal protection (safeguard of justice, guardianship, tutorship) and persons deprived of their liberty.
15 Years
ALL
Yes
Sponsors
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Rennes University Hospital
OTHER
Responsible Party
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Principal Investigators
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Xavier MD RAVALEC
Role: PRINCIPAL_INVESTIGATOR
Rennes University Hospital
Locations
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CREPS de Wattignies
Wattignies, Hauts-de-France, France
Countries
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Other Identifiers
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35RC17_8823_IODPR
Identifier Type: -
Identifier Source: org_study_id
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